ClinVar Miner

Submissions for variant NM_001379610.1(SPINK1):c.194+19T>G

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002913778 SCV003254458 likely benign Hereditary pancreatitis 2022-10-17 criteria provided, single submitter clinical testing

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